Clinical Trial Associate

ICON plc • Montreal, QC

3d

About The Position

Clinical Trial Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patient faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Clinical Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. What You Will Do: You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines. Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies. Overseeing site management and monitoring to ensure data integrity and compliance with study protocols. Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards. Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges. Your Profile: You will have a strong foundation in clinical coordination, with the experience to work independently and guide others. En tant qu’Attaché(e) de Recherche Clinique (Clinical Trial Associate) chez ICON, vous superviserez et soutiendrez la mise en œuvre des essais cliniques, en garantissant les plus hauts standards de qualité, de conformité et d’efficacité. Vos missions : Vous serez en charge des activités de coordination clinique nécessitant une expertise technique, avec un fort accent sur la qualité et l’amélioration continue. Vos principales responsabilités incluent : Assurer la gestion et la coordination des activités liées aux essais cliniques afin de garantir le respect des protocoles, des exigences réglementaires et des délais des projets. Collaborer avec des équipes pluridisciplinaires pour résoudre les problématiques liées aux essais, optimiser les processus et assurer une exécution efficace des études. Superviser la gestion des sites et le suivi (monitoring) afin de garantir l’intégrité des données et la conformité aux protocoles. Fournir un accompagnement et un support aux équipes cliniques et aux investigateurs, en veillant au respect des bonnes pratiques et des normes réglementaires. Suivre et analyser l’avancement des essais, identifier les risques potentiels et mettre en œuvre des stratégies pour anticiper et atténuer les difficultés. Votre profil : Vous disposez de solides bases en coordination clinique, avec la capacité de travailler de manière autonome et d’accompagner d’autres collaborateurs.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
• Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.

Responsibilities

• Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
• Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
• Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
• Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
• Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level